PHOENIX MEDICAL SOLUTIONS

FDA Device Registration & Listing · Hunt Valley, MD, US · Registration 3015824790

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015824790
FEI Number
3015824790
Entity Name
PHOENIX MEDICAL SOLUTIONS
City/State/Country
Hunt Valley, MD, US
Establishment Address
10955 Golden West Dr., Ste B, Hunt Valley, MD 21031, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Phoenix Medical Solutions (Owner Number: 10062327)
Owner / Operator Contact Address
10955 Golden West Dr, Ste B, Hunt Valley, MD 21031, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Roll A Bout Walker

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITJ Walker, Mechanical Physical Medicine Class 1 890.3825 2020-01-13

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Phoenix Medical Solutions
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015824790. Last updated year: 2026. Please use registration number 3015824790 when referencing this establishment in official correspondence.
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